(9S)-Cinchonan-9-ol sulfate (2:1)

Modify Date: 2025-08-21 20:33:08

(9S)-Cinchonan-9-ol sulfate (2:1) Structure
(9S)-Cinchonan-9-ol sulfate (2:1) structure
Common Name (9S)-Cinchonan-9-ol sulfate (2:1)
CAS Number 5949-16-6 Molecular Weight 686.860
Density 1.61g/cm3 Boiling Point 169 °C(lit.)
Molecular Formula C38H46N4O6S Melting Point 38-40 °C(lit.)
MSDS USA Flash Point 148 °F

 Names

Name Cinchonine Sulfate Dihydrate
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.61g/cm3
Boiling Point 169 °C(lit.)
Melting Point 38-40 °C(lit.)
Molecular Formula C38H46N4O6S
Molecular Weight 686.860
Flash Point 148 °F
Exact Mass 686.313782
PSA 155.70000
LogP 6.63300
Index of Refraction 1.717

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
GD3800000
CAS REGISTRY NUMBER :
5949-16-6
LAST UPDATED :
198708
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C19-H22-N2-O.1/2H2-O4-S
MOLECULAR WEIGHT :
343.43

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
800 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPETAB Journal of Pharmacology and Experimental Therapeutics. (Williams & Wilkins Co., 428 E. Preston St., Baltimore, MD 21202) V.1- 1909/10- Volume(issue)/page/year: 78,159,1943

 Safety Information

Hazard Codes Xi
Risk Phrases R36/37/38
Safety Phrases 26-36
RIDADR 1544
WGK Germany 3
RTECS GD3800000
Packaging Group III
Hazard Class 6.1(b)

 Articles24

More Articles
Mutation in the Plasmodium falciparum CRT protein determines the stereospecific activity of antimalarial cinchona alkaloids.

Antimicrob. Agents Chemother. 56(10) , 5356-64, (2012)

The Cinchona alkaloids are quinoline aminoalcohols that occur as diastereomer pairs, typified by (-)-quinine and (+)-quinidine. The potency of (+)-isomers is greater than the (-)-isomers in vitro and ...

A theoretical investigation on the Strecker reaction catalyzed by a Ti(IV)-complex catalyst generated from a cinchona alkaloid, achiral substituted 2,2'-biphenol, and tetraisopropyl titanate.

Chemistry 19(5) , 1637-46, (2013)

The mechanism and the origin of selectivity of the asymmetric Strecker reaction catalyzed by a Ti(IV)-complex catalyst generated from a cinchona alkaloid, achiral substituted 2,2'-biphenol, and tetrai...

Organocatalytic asymmetric conjugate addition of 3-monosubstituted oxindoles to (E)-1,4-diaryl-2-buten-1,4-diones: a strategy for the indirect enantioselective furanylation and pyrrolylation of 3-alkyloxindoles.

Chemistry 18(21) , 6679-87, (2012)

An asymmetric conjugate addition of 3-monosubstituted oxindoles to a range of (E)-1,4-diaryl-2-buten-1,4-diones, catalyzed by commercially available cinchonine, is described. This organocatalytic asym...

 Synonyms

Cinchonan-9-ol, (9S)-, sulfate (2:1) (salt)
(9S)-Cinchonan-9-ol sulfate (2:1)
EINECS 227-708-4
MFCD00035639
cinchonine sulfate
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here


Get all suppliers and price by the below link:

(9S)-Cinchonan-9-ol sulfate (2:1) suppliers

(9S)-Cinchonan-9-ol sulfate (2:1) price